Canonical Allele Identifier: CA403988157

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464794C>A (hg19) ; chr19:g.10354118C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354118C>A , CM000681.2:g.10354118C>A	GRCh38
NC_000019.9:g.10464794C>A , CM000681.1:g.10464794C>A	GRCh37
NC_000019.8:g.10325794C>A	NCBI36
NG_007872.1:g.31455G>T , LRG_121:g.31455G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1181G>T	ENSP00000514307.1:n.*1181G>T
ENST00000525976.6:c.2832G>T	ENSP00000434831.2:p.Trp944Cys
ENST00000527481.3:c.2832G>T	ENSP00000466340.2:p.Trp944Cys
ENST00000529370.6:n.4208G>T
ENST00000529739.2:n.3246G>T
ENST00000530829.2:c.*2383G>T	ENSP00000436826.2:n.*2383G>T
ENST00000531836.6:c.2832G>T	ENSP00000436175.2:p.Trp944Cys
ENST00000533334.2:c.*874G>T	ENSP00000432320.2:n.*874G>T
ENST00000534228.2:n.4291G>T
ENST00000699354.1:n.934G>T
ENST00000699355.1:c.*1937G>T	ENSP00000514328.1:n.*1937G>T
ENST00000699356.1:n.3246G>T
ENST00000699357.1:n.4291G>T
ENST00000699358.1:c.2832G>T	ENSP00000514329.1:p.Trp944Cys
ENST00000699359.1:c.38G>T
ENST00000699360.1:c.2832G>T	ENSP00000514331.1:p.Trp944Cys
ENST00000699368.1:c.36G>T	ENSP00000514335.1:p.Trp12Cys
ENST00000525621.6:c.2832G>T MANE Select	ENSP00000431885.1:p.Trp944Cys
ENST00000264818.10:c.2832G>T	ENSP00000264818.6:p.Trp944Cys
ENST00000524462.5:c.2277G>T	ENSP00000433203.1:p.Trp759Cys
ENST00000525621.5:c.2832G>T	ENSP00000431885.1:p.Trp944Cys
ENST00000527481.2:c.128G>T
ENST00000529412.1:n.504G>T
ENST00000530560.5:c.261G>T	ENSP00000465291.1:p.Trp87Cys
NM_003331.4:c.2832G>T , LRG_121t1:c.2832G>T	NP_003322.3:p.Trp944Cys
XM_011528245.1:c.2832G>T	XP_011526547.1:p.Trp944Cys
XM_011528246.1:c.2535G>T	XP_011526548.1:p.Trp845Cys
XM_011528247.1:c.2535G>T	XP_011526549.1:p.Trp845Cys
XM_011528248.1:c.2832G>T	XP_011526550.1:p.Trp944Cys
XM_011528249.1:c.1506G>T	XP_011526551.1:p.Trp502Cys
XM_011528251.1:c.1089G>T	XP_011526553.1:p.Trp363Cys
XM_011528246.3:c.2535G>T	XP_011526548.1:p.Trp845Cys
XM_011528249.2:c.1506G>T	XP_011526551.1:p.Trp502Cys
XR_001753750.1:n.2989G>T
XR_001753751.1:n.2989G>T
XR_002958353.1:n.3915G>T
NM_003331.5:c.2832G>T MANE Select	NP_003322.3:p.Trp944Cys
NM_001385197.1:c.2832G>T	NP_001372126.1:p.Trp944Cys
NM_001385198.1:c.2832G>T	NP_001372127.1:p.Trp944Cys
NM_001385199.1:c.2646G>T	NP_001372128.1:p.Trp882Cys
NM_001385200.1:c.2829G>T	NP_001372129.1:p.Trp943Cys
NM_001385201.1:c.2634G>T	NP_001372130.1:p.Trp878Cys
NM_001385202.1:c.2748G>T	NP_001372131.1:p.Trp916Cys
NM_001385203.1:c.2913G>T	NP_001372132.1:p.Trp971Cys
NM_001385204.1:c.3042G>T	NP_001372133.1:p.Trp1014Cys
NM_001385205.1:c.2742G>T	NP_001372134.1:p.Trp914Cys
NM_001385206.1:c.2706G>T	NP_001372135.1:p.Trp902Cys
NM_001385207.1:c.2814G>T	NP_001372136.1:p.Trp938Cys